Efficient Synthesis of O-Linked Glycopeptide by a Transglycosylation Using Endo .ALPHA.-N-Acetylgalactosaminidase from Streptomyces sp.
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- AJISAKA Katsumi
- Nutrition Science Institute, Meiji Milk Products Co. Ltd.
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- MIYASATO Mariko
- Nutrition Science Institute, Meiji Milk Products Co. Ltd.
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- ISHII-KARAKASA Ikuko
- Department of Biochemistry, School of Medicine, Kitasato University
Bibliographic Information
- Other Title
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- Efficient Synthesis of O-Linked Glycopeptide by a Transglycosylation Using Endo α-N-Acetylgalactosaminidase from Streptomyces sp
- Efficient Synthesis of O Linked Glycopeptide by a Transglycosylation Using Endo アルファ N Acetylgalactosaminidase from Streptomyces sp
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Abstract
Galβ-(1→3)-GalNAc-linked hexapeptide was synthe-sized by a transglycosylation using Galβ-(1→3)-Gal-NAcβ-pNP as a donor and a serine-containing hexapeptide as an acceptor using endo GalNAc-ase from Streptomyces sp.. The Galβ-(1→3)-GalNAc residue was transferred to the hydroxyl group of the serine residue of the peptide. The total yield of the glycopeptide via this process was better than that of the chemoenzymatic method. This process was confirmed to be a versatile method for the synthesis of O-linked glycopeptides.
Journal
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- Bioscience, Biotechnology, and Biochemistry
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Bioscience, Biotechnology, and Biochemistry 65 (5), 1240-1243, 2001
Japan Society for Bioscience, Biotechnology, and Agrochemistry
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Details 詳細情報について
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- CRID
- 1390282681452827776
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- NII Article ID
- 110002680425
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- NII Book ID
- AA10824164
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- COI
- 1:CAS:528:DC%2BD3MXktFaitrY%3D
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- ISSN
- 13476947
- 09168451
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- NDL BIB ID
- 5783003
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- PubMed
- 11440149
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed